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FDA Inspection 1028622 — Raimund Weitgasser, MD

Raimund Weitgasser, MD — FEI 3013836802

The FDA completed an inspection of Raimund Weitgasser, MD on Sep 29, 2017 in Salzburg. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection details

Classification
No Action Indicated (NAI)
End Date
Sep 29, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Salzburg (Austria)

Additional details

Clinical Investigator (CI)

Facility

FDA data resources

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.